Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®

Cell part

Cell part

  • Apical part of cell
    • USH1C: Usher syndrome 1C (autosomal recessive, severe)
    • Apical plasma membrane
      • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
      • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
      • SLC26A4: solute carrier family 26, member 4
      • SLC46A1: solute carrier family 46 (folate transporter), member 1
  • Basal part of cell
    • Basal plasma membrane
      • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • Cell division site
    • Cell division site part
      • MEN1: multiple endocrine neoplasia I
  • Cell division site part
    • Cleavage furrow
      • MEN1: multiple endocrine neoplasia I
  • Cell fraction
  • Cell leading edge
    • Lamellipodium
      • ALS2: amyotrophic lateral sclerosis 2 (juvenile)
      • FGD1: FYVE, RhoGEF and PH domain containing 1
      • TSC1: tuberous sclerosis 1
    • Ruffle
      • ALS2: amyotrophic lateral sclerosis 2 (juvenile)
      • FGD1: FYVE, RhoGEF and PH domain containing 1
  • Cell projection
  • Cell projection part
    • Cell projection cytoplasm
      • SOD1: superoxide dismutase 1, soluble
    • Cilium part
      • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
    • Microtubule basal body
      • PKD2: polycystic kidney disease 2 (autosomal dominant)
      • PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
  • Cell soma
  • Cell surface
  • Endomembrane system
    • Golgi membrane
      • ARFGEF2: ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
      • CLN3: ceroid-lipofuscinosis, neuronal 3
      • GJA1: gap junction protein, alpha 1, 43kDa
      • GJB2: gap junction protein, beta 2, 26kDa
      • GNAS: GNAS complex locus
      • LDLRAP1: low density lipoprotein receptor adaptor protein 1
    • Nuclear envelope
      • DHCR7: 7-dehydrocholesterol reductase
      • MYO6: myosin VI
      • NPC1: Niemann-Pick disease, type C1
      • PSEN1: presenilin 1
    • Nuclear envelope-endoplasmic reticulum network
    • Vesicle membrane
      • APOB: apolipoprotein B (including Ag(x) antigen)
      • GJA1: gap junction protein, alpha 1, 43kDa
      • KIF1B: kinesin family member 1B
      • LDLR: low density lipoprotein receptor
      • LDLRAP1: low density lipoprotein receptor adaptor protein 1
      • TH: tyrosine hydroxylase
  • Intracellular
    • MKKS: McKusick-Kaufman syndrome
    • NYX: nyctalopin
    • TNXB: tenascin XB
    • VPS13A: vacuolar protein sorting 13 homolog A (S. cerevisiae)
  • Intracellular part
  • Membrane
  • Membrane part
  • Perikaryon
    • TH: tyrosine hydroxylase
  • Photoreceptor inner segment
    • GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
    • MYO7A: myosin VIIA
  • Site of polarized growth
    • Growth cone
      • ANG: angiogenin, ribonuclease, RNase A family, 5
      • SNCA: synuclein, alpha (non A4 component of amyloid precursor)

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference. (June 2009).

 
Published: October 30, 2009